Gene >> CERK
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000216264 |
| Start |
46720983:46720983(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.175G>A |
| AA Mutation |
p.Ala59Thr(p.A59T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000216264 |
| Start |
46691692:46691692(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs201852137
|
| CDS Mutation |
c.1212C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |